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Structure of 62077-26-3
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3,6-Dichloro-2-methylaniline features a chlorine-substituted aromatic ring with a methyl group at the ortho position, delivering enhanced electron-withdrawal and steric shielding. This configuration supports stable coupling reactions in pharmaceutical intermediates and agrochemical synthesis under standard conditions.
3,6-Dichloro-2-methylaniline serves as a valuable building block in medicinal chemistry and agrochemical synthesis, offering a highly functionalized aromatic scaffold with orthogonal reactivity. The electron-deficient aryl ring facilitates electrophilic substitution, while the primary amine enables coupling reactions (e.g., Suzuki, Buchwald–Hartwig). Bench-stable and readily purified by recrystallization, it functions effectively in multi-step syntheses requiring precise regiocontrol and compatibility with diverse protecting groups.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: